GB2085582A - Indicator - Google Patents
Indicator Download PDFInfo
- Publication number
- GB2085582A GB2085582A GB8126553A GB8126553A GB2085582A GB 2085582 A GB2085582 A GB 2085582A GB 8126553 A GB8126553 A GB 8126553A GB 8126553 A GB8126553 A GB 8126553A GB 2085582 A GB2085582 A GB 2085582A
- Authority
- GB
- United Kingdom
- Prior art keywords
- indicator
- substance
- product according
- atmosphere
- active agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N17/00—Investigating resistance of materials to the weather, to corrosion, or to light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
- G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
Abstract
An indicator composition for indicating the useful life of a product which releases an active agent into the atmosphere, e.g., an air freshener, insecticide or corrosion inhibitor comprises a substance, e.g., a dye, which becomes oxidised and so changes colour on exposure to the atmosphere and means for inhibiting the rate at which such oxidation occurs, whereby the said colour change takes place over a predetermined time. The oxidation inhibitor may be a barrier layer such as a polymer film, an antioxidant or a reducing agent. Indicators exemplified comprise a dye and sodium dithionite reducing agent.
Description
1
GB 2 085 582 A 1
SPECIFICATION
Improved Indicator System for Useful Life of Products which Release Active Agents into the Atmosphere
5 This invention relates to an indicator particularly although not exclusively for a product containing a composition such as an air-freshener, insecticide or a vapour phase corrosion inhibitor, which releases an active agent into the *1 o atmosphere, to indicate the useful life of such a product. The invention also relates to a product of the above mentioned kind including such an indicator.
With certain conventional products of this kind, 15 the composition eventually decomposes so that it is possible to see when the product needs to be replaced. Otherwise detection of the useful life is not possible except, when the active agent has a distinctive odour, by smell. However, even testing 20 by smell is imprecise since the active agent may be masked by other more powerful odours.
One object of the present invention is to provide a more reliable and easily discernable indication of the useful life of these products. 25 Various colour change indicator systems are known for example acid-base indicators for indicating pH, but it has not hitherto been possible to provide a time span indicator suitable, for example, for indicating the useful life of 30 products of the kind referred to, by colour change which can be related to the exhaustion of the products active agent into the atmosphere. However, market research has indicated that there is a substantial demand for such an 35 indicator.
According to one aspect of the invention there is provided an indicator comprising a substance which becomes oxidised and so changes colour on exposure to the atmosphere and means for 40 inhibiting the rate at which such oxidation occurs, whereby the said colour change takes place over a predetermined time.
The choice of a colour change caused by oxidation of the substance concerned, which is 45 preferably a dye, for example, a vat dye, has particular advantage since oxygen is ubiquitous and generally present in the atmosphere in constant proportions.
Although indicators according to the present 50 invention may be used in general to indicate the 4 expiry of any period of time selected or predetermined by suitably controlling the oxidation rate, they may, with particular advantage, be used to indicate the useful life of 55 products of the kind referred to above, containing a composition which releases an active agent into the atmosphere.
According to another aspect of the invention there is therefore provided a product comprising a 60 composition capable of gradually releasing an active agent into the atmosphere on exposure thereto, and an indicator comprising a substance which becomes oxidised and so changes colour on exposure to the atmosphere and means for
65 inhibiting the rate at which such oxidation occurs, whereby the said colour change takes place over a predetermined time.
Preferably, the colour change becomes complete as the active agent becomes exhausted. 70 Any increase or decrease in the depletion rate of the product as a result of temperature variations will be at Jeast partially compensated for by a corresponding increase or decrease in the rate of oxidation of the said substance. 75 The substance which changes colour may, for example, be dispersed in a liquid, gel, solid or polymer, or is applied to a substrate. The product may also be present in the same liquid, gel, solid or polymer, or be applied to the same or different 80 substance. Various types of inhibiting means may be employed. For example, the inhibiting means may comprise a reducing agent or antioxidant, or alternatively or additionally a barrier layer physically separating the substance which 85 changes colour from the atmosphere, but permeable to oxygen at a predetermined rate.
In this latter case, the barrier layer may be a polymer film or a lacquer film, or the barrier layer may form at least a part of a container for the 90 indicator or product. In these cases the product may also be present in the film or container.
In certain preferred embodiments, the substance which changes colour is a vat dye.
The colour change may occur at any selected 95 stage in depletion of the active agent but preferably occurs when substantially all of the active agent is expended. The substance may either be dissolved or otherwise dispersed in a suitable liquid, gel, solid or polymer (e.g. polyvinyl 100 pyrrolidene) medium or be absorbed into or otherwise applied to a substrate of, for example textile and/or paper material. If the substance is a vat dye, the reduced form of this is rapidly oxidised to the quinonoid form, this being a well 105 recognised phenomenon which is the basis of the vat dyeing process for cotton and other textiles.
The present invention relies upon controlling the rate at which the oxidation reaction proceeds and this may be achieved in a variety of ways, for 110 example, chemically, by the addition of suitable antioxidants to the substance or by disposing the substance in a reducing environment (if necessary in the presence of an alkali, depending on the type of dye used) which in addition to improving the 115 stability of the substance acts to slow down the oxidation rate if it is dispersed in a gel, or other matrix or is absorbed on a carrier substrate.
We prefer, however, to control the oxidation reaction by means of a barrier layer physically 120 separating the substance from the atmosphere but permeable to oxygen at a predetermined rate selected so as to regulate the access of oxygen from the air and hence control the colour change ' of the substance over a predetermined period of 125 time. This period of time may usefully be extended to be a number of days, weeks or even months. Suitable barrier materials comprise, for example, polyethylene, polypropylene, polyester, polyamide, cellulose, polyvinyl chloride,
2
GB 2 085 582 A 2
polyvinylidene chloride, or similar polymer films and including copolymers of the above or lacquered films.
The gauge or thickness of the chosen barrier 5 layer may be selected to suit the desired product life, e.g. a thin polyethylene film might be chosen where a short product life of hours or a few days is required, whereas a more substantial film of, for example, polyethylene/polyester colaminate might 10 be chosen for a product intended to have a life expectancy of a number of weeks.
An oxgyen permeability of as low as 0.001 cm3/cm2 min (at a pressure of 1 Kg/cm2) may be achieved using polyethylene/polyester composite 15 films whereas a film of microporous polypropylene can be produced having an oxygen permeability in the range 3 to 5 cm3/cm2/min.
In the case of co-extruded biaxialiy-oriented polypropylene film which we have found 20 particularly suitable, the variation in oxygen permeability bears a substantially linear relationship to the thickness of the film. This enables accurate control of the oxidation rate and hence timing of the colour change. Although with 25 products of the kind referred to, matching of the oxidation rate to the rate of depletion of the active agent is basically an empirical process, accurate matching is nevertheless possible. When the substance is dispersed in a solution, gel or 30 polymer matrix the barrier layer may be in the form of, or form part of, a container therefore having the required oxygen permeability and being transparent or translucent whereby the colour change is visible. Where the product is an 35 air freshener this may take the form of a thermoplastic shape e.g. disc containing volatile perfume components in which disc is a window comprising two strips of thermoplastic transparent film containing the substance in an 40 aqueous gel. The oxygen permeability of the transparent film is chosen to permit the colour change to take place over a period related to the loss of perfume from the bulk of the disc.
It will be understood, that the product may 45 contain compositions other than air fresheners; for example; insecticides, a vapour phase corrosion inhibitor, a microbiocide or a timber preservative.
The active agent also may be dissolved or 50 dispersed in the solution, gel or polymer matrix.
Alternatively the active agent is absorbed into or otherwise applied to a substrate comprising an absorbent material such as a woven or non-woven paper and/or textile fabric. In one 55 embodiment the colour change indicator system is attached to the substrate and preferably comprises the above described oxygen permeable envelope containing the gel in which the reduced substance is dispersed.
60 In a preferred embodiment both the active agent and the reduced dye or dye together with a reducing agent are applied to a substrate preferably by absorbtion or impregnation and in either the same or different areas of the substrate. 65 Control of the dye oxidation reaction is best achieved by coating (or colaminating) the substrate after the dye and the active agent have been applied, with a film of oxygen permeable polymeric material which is also permeable to the active agent allowing release thereof into the atmosphere. To avoid oxidation of the reduced dye prior to application of permeable film the impregnated substrate may be stored and * subsequently processed in an inert atmosphere. Alternatively, after impregnation of the substrate,
the dye and the permeable film may be applied "* simultaneously by dipping the substrate in a bath of a solution of the reduced vat dye or vat dye and reducing agent in the polymeric material so that the reduced form of vat dye is absorbed into the substrate and immediately covered with a film of polymeric material which is subsequently dried and/or cured.
In a further embodiment, the reduced dye may be applied to the substrate in the form of microcapsules containing the reduced dye, the walls of the micro-capsules forming the required oxygen permeable barrier. In such an embodiment, the active principle may be contained on the substrate or within the microcapsules. The *
microcapsule walls may be of a wide variety of materials, for example gelatin, alginate, polyvinyl alchohol and other water soluble materials or water insoluble thermoplastics polymers in the case of microcapsules produced by co-acervation.
As stated above the dye is preferably a vat dye.
Examples of suitable dyes are: Indigo, Alizarins,
Solanthrene Bordeaux F2R, Caledon BlueXRC,
Ciba Blue 2RH, Cibanone Red 6B, Cibanone Yellow GC.
The reducing system utilised may comprise an alkali and a reducing agent, the choice of which is largely influenced by the dye being used. The concentration of dye, alkali, and reducing agent and the respective ratios of these agents may usefully be varied over a wide range to influence the rate of colour change. The alkali may be chosen from among ammonium or alkali metal hydroxides, carbonates, phosphates or other suitable alkali metal salts, or organic alkalis such i as amines, alkanolamines etc. or may in certain cases advantageously be an alkaline structuring agent such as a synthetic hectorite. The reducing agent is preferably sodium dithionite, but other agents such as sodium borohydride may also be*
utilised.
One example of an indicator composition according to the present invention contains
1 —5 parts by weight of reducing agent (e.g.
sodium dithionite)
0.05—5 parts by weight of dye (e.g. Cibanone Yellow GC
0.1—5 parts by weight of alkali (e.g. NaOH)
If the remainder is water this will produce a liquid composition containing the reduced form of dye which can be enclosed within an envelope of oxygen permeable material or may be used to dye a substrate such as a fabric, which is subsequently coated with a suitable film selected to produce the desired oxidation rate.
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3
GB 2 085 582 A 3
With the addition of 0.05—5 p.b.w. of a structuring agent such as Agar to the above composition a gel is produced and this may, but need not necessarily be, enclosed within an 5 oxygen permeable film selected as described above.
One particular indicator contains 1 p.b.w. Sodium dithionite (reducing agent) 0.05—1 p.b.w. dye 10 0.3 p.b.w. Na OH 2.5 p.b.w. Agar remainder water.
This indicator can be prepared by dispersing the Agar in water and heating to dissolve the agar 1 5 before adding the reducing agent together with the dye. On adding the alkali and mixing until it dissolves there is a colour change as the dye is converted to the reduced form. The resulting gel is then enclosed within a polypropylene or 20 polyethylene capsule having an oxygen permeability of 1 cm3/cm2/min to produce an indicator which will exhibit a colour change after a predetermined time in the range 3 to 7 days.
Claims (11)
- Claims25 1. An indicator comprising a substance which becomes oxidised and so changes colour on exposure to the atmosphere and means for inhibiting the rate at which such oxidation occurs, whereby the said colour change takes place over 3Q a predetermined time.
- 2. A product comprising a composition capable of gradually releasing an active agent into the atmosphere on exposure thereto, and an indicator comprising a substance which becomes oxidised 35 and so changes colour on exposure to the atmosphere and means for inhibiting the rate at which such oxidation occurs, whereby the said colour change takes place over a predetermined time.40
- 3. An indicator or product according to claim 1 or claim 2 respectively, wherein the colour change becomes complete as the active agent becomes exhausted.
- 4. An indicator or product according to claim 145 or claim 2 respectively, or claim 3, wherein the substance is dispersed in a liquid, gel, or polymer, or is applied to a substrate.
- 5. An indicator or product according to claim 1 or claim 2 respectively, or according to claim 3 or50 claim 4 wherein the inhibiting means comprises a reducing agent or antioxidant.
- 6. An indicator or product according to claim 1 or claim 2 respectively, or according to claim 3 or claim 4, wherein the inhibiting means comprises a55 barrier layer physically separating the substance from the atmosphere, but permeable to oxygen at a predetermined rate.
- 7. An indicator or product according to claim 6, wherein the barrier layer is a polymer film or a60 lacquer film.
- 8. An indicator or product according to claim 6, wherein the barrier layer forms at least a part of a container for the indicator or product.
- 9. An indicator or product according to claim 165 or claim 2 respectively, or to claims 3 to 8,wherein the substance is a vat dye.
- 10. A product according to claim 2 wherein the active agent is present in the same or in a different liquid, gel, or polymer or is applied to the70 same or to a different substance.
- 11. A product according to claim 7 or claim 8, wherein the active agent is in the film or in the container.Printed for Her Majesty's Stationery Office by the Courier Press, Leamington Spa, 1982. Published by the Patent Office, 25 Southampton Buildings, London, WC2A 1 AY, from which copies may be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8028307 | 1980-09-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB2085582A true GB2085582A (en) | 1982-04-28 |
Family
ID=10515790
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8126553A Withdrawn GB2085582A (en) | 1980-09-02 | 1981-09-02 | Indicator |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0047101A3 (en) |
JP (1) | JPS57168158A (en) |
KR (1) | KR830008166A (en) |
AU (1) | AU7445481A (en) |
BR (1) | BR8105631A (en) |
DK (1) | DK386481A (en) |
ES (1) | ES8303771A1 (en) |
FI (1) | FI812668L (en) |
GB (1) | GB2085582A (en) |
GR (1) | GR75763B (en) |
NO (1) | NO812959L (en) |
PT (1) | PT73609B (en) |
ZA (1) | ZA815943B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5278132A (en) * | 1986-02-11 | 1994-01-11 | Gouws & Scheepers (Propietary) Ltd. | Agricultural compounds |
US6561008B1 (en) * | 1999-10-28 | 2003-05-13 | Guelph Food Technology Centre | Determination of oxygen permeation into containers |
GB2408047A (en) * | 2003-11-12 | 2005-05-18 | Colormatrix Europe Ltd | Colourant for use in thermoplastic compositions |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4533640A (en) * | 1984-02-21 | 1985-08-06 | Shafer Jules A | Accumulated thermal exposure responder and method of use |
EP0231499A1 (en) * | 1986-01-02 | 1987-08-12 | Allied Corporation | Activatable time-temperature indicator |
GB2209942A (en) * | 1987-09-23 | 1989-06-01 | Johnson & Son Inc S C | Air refreshening compositions containing indicators |
US7651989B2 (en) * | 2003-08-29 | 2010-01-26 | Kimberly-Clark Worldwide, Inc. | Single phase color change agents |
US8067350B2 (en) | 2005-12-15 | 2011-11-29 | Kimberly-Clark Worldwide, Inc. | Color changing cleansing composition |
CN101324530B (en) * | 2007-06-15 | 2010-07-21 | 林唯芳 | Time process indicating device and its forming method |
JP4757931B2 (en) * | 2009-05-22 | 2011-08-24 | 内橋エステック株式会社 | Protective element |
US20180184876A1 (en) * | 2015-05-26 | 2018-07-05 | Kimberly-Clark Worldwide, Inc. | Wiper with use indicator |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062649A (en) * | 1974-04-29 | 1977-12-13 | Shell Oil Company | Depletion indicator for controlled-release pesticide formulations |
GB1581333A (en) * | 1976-07-02 | 1980-12-10 | Unilever Ltd | Colour change systems |
US4169811A (en) * | 1977-03-23 | 1979-10-02 | Mitsubishi Gas Chemical Co., Inc. | Oxygen indicator |
JPS54134492A (en) * | 1978-04-10 | 1979-10-18 | Dainichiseika Color Chem | Composite substance for indicating oxygennsensitive indicating |
JPS5530665A (en) * | 1978-08-26 | 1980-03-04 | Ishikawajima Harima Heavy Ind | Method of improving filteration properties of radioactive filter sludge waste |
US4248597A (en) * | 1978-12-12 | 1981-02-03 | Akzona Incorporated | Time watch or depletion indicator for removable substances |
-
1981
- 1981-08-19 EP EP81303779A patent/EP0047101A3/en not_active Withdrawn
- 1981-08-24 AU AU74454/81A patent/AU7445481A/en not_active Abandoned
- 1981-08-25 GR GR65869A patent/GR75763B/el unknown
- 1981-08-27 ZA ZA815943A patent/ZA815943B/en unknown
- 1981-08-28 ES ES505028A patent/ES8303771A1/en not_active Expired
- 1981-08-28 FI FI812668A patent/FI812668L/en not_active Application Discontinuation
- 1981-08-31 JP JP56136925A patent/JPS57168158A/en active Pending
- 1981-09-01 DK DK386481A patent/DK386481A/en not_active Application Discontinuation
- 1981-09-01 PT PT73609A patent/PT73609B/en unknown
- 1981-09-01 NO NO812959A patent/NO812959L/en unknown
- 1981-09-02 BR BR8105631A patent/BR8105631A/en unknown
- 1981-09-02 KR KR1019810003277A patent/KR830008166A/en unknown
- 1981-09-02 GB GB8126553A patent/GB2085582A/en not_active Withdrawn
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5278132A (en) * | 1986-02-11 | 1994-01-11 | Gouws & Scheepers (Propietary) Ltd. | Agricultural compounds |
US5514639A (en) * | 1986-02-11 | 1996-05-07 | Gouws & Scheepers (Proprietary) Limited | Agricultural compositions comprising pH buffers, pH indicators, and pH sensitive agrochemicals |
US6561008B1 (en) * | 1999-10-28 | 2003-05-13 | Guelph Food Technology Centre | Determination of oxygen permeation into containers |
GB2408047A (en) * | 2003-11-12 | 2005-05-18 | Colormatrix Europe Ltd | Colourant for use in thermoplastic compositions |
Also Published As
Publication number | Publication date |
---|---|
PT73609B (en) | 1983-10-19 |
KR830008166A (en) | 1983-11-16 |
EP0047101A3 (en) | 1982-03-24 |
ZA815943B (en) | 1982-08-25 |
GR75763B (en) | 1984-08-02 |
AU7445481A (en) | 1982-03-11 |
NO812959L (en) | 1982-03-03 |
JPS57168158A (en) | 1982-10-16 |
ES505028A0 (en) | 1983-02-01 |
PT73609A (en) | 1981-10-01 |
DK386481A (en) | 1982-03-03 |
EP0047101A2 (en) | 1982-03-10 |
BR8105631A (en) | 1982-05-18 |
ES8303771A1 (en) | 1983-02-01 |
FI812668L (en) | 1982-03-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |